ENST00000700061.1:c.630T>G
|
|
|
ENST00000700062.1:c.630T>G
|
|
|
ENST00000700065.1:n.2546T>G
|
|
|
ENST00000700066.1:c.2050T>G
|
ENSP00000514780.1:p.Trp684Gly
|
|
ENST00000281513.10:c.2533T>G
MANE Select
|
ENSP00000281513.5:p.Trp845Gly
|
|
ENST00000281513.9:c.2533T>G
|
ENSP00000281513.5:p.Trp845Gly
|
|
ENST00000441755.5:c.34T>G
|
ENSP00000396501.1:p.Trp12Gly
|
|
ENST00000442506.5:c.36T>G
|
|
|
NM_015909.3:c.2533T>G
|
NP_056993.2:p.Trp845Gly
|
|
NR_052013.2:n.2577T>G
|
|
|
XM_011510357.1:c.2404T>G
|
XP_011508659.1:p.Trp802Gly
|
|
XM_011510358.1:c.2533T>G
|
XP_011508660.1:p.Trp845Gly
|
|
XM_011510359.1:c.1894T>G
|
XP_011508661.1:p.Trp632Gly
|
|
XM_011510360.1:c.334T>G
|
XP_011508662.1:p.Trp112Gly
|
|
XM_011510361.1:c.325T>G
|
XP_011508663.1:p.Trp109Gly
|
|
XM_011510357.2:c.2404T>G
|
XP_011508659.1:p.Trp802Gly
|
|
XM_011510358.2:c.2533T>G
|
XP_011508660.1:p.Trp845Gly
|
|
XM_011510360.2:c.334T>G
|
XP_011508662.1:p.Trp112Gly
|
|
XM_011510361.2:c.325T>G
|
XP_011508663.1:p.Trp109Gly
|
|
XM_017004317.1:c.2533T>G
|
XP_016859806.1:p.Trp845Gly
|
|
XM_024452961.1:c.1894T>G
|
XP_024308729.1:p.Trp632Gly
|
|
NM_015909.4:c.2533T>G
MANE Select
|
NP_056993.2:p.Trp845Gly
|
|
NR_052013.3:n.2563T>G
|
|
|